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Class I: serious health riskTerminated

Tamarack ECLIPSE Kratom Premium Maeng Da Recall

ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tam…

Tamarack, Inc. · Roy, UT

Risk level
Class I
Reported by FDA
Apr 11, 2018
Recall ID
F-0992-2018
Check your lot numberHow we source this data

Summary

Tamarack recalled ECLIPSE Kratom Premium Maeng Da starting Mar 19, 2018. The FDA classified it as Class I (serious health risk) and published enforcement report F-0992-2018 on Apr 11, 2018. Reason: Tamarack Inc. is recalling Eclipse Kratom-containing powder products because it may be contaminated with Salmonella. Status: Terminated.

Why it was recalled

Tamarack Inc. is recalling Eclipse Kratom-containing powder products because it may be contaminated with Salmonella.

Product description

ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tamarack Inc. Cheyenne, WY

Lot numbers, UPCs & expiration codes

All products on market.

Where it was sold

Distributed to retail stores in Utah. No foreign/VA/govt/military consignees.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0992-2018
Classification
Class I
Status
Terminated
Recall initiated
Mar 19, 2018
FDA report date
Apr 11, 2018
Quantity
120 units
Recall type
Voluntary: Firm initiated
Recalling firm
Tamarack, Inc.

Original FDA data

Every field from FDA enforcement report F-0992-2018, exactly as published.

Show all FDA fields
City
Roy
State
UT
Status
Terminated
Country
United States
Event ID
79565
Address
3750 Midland Dr
Code information
All products on market.
Postal code
84067-9764
Report date
Apr 11, 2018
Product type
Food
Recall number
F-0992-2018
Classification
Class I
Recalling firm
Tamarack, Inc.
Product quantity
120 units
Termination date
Mar 11, 2020
Reason for recall
Tamarack Inc. is recalling Eclipse Kratom-containing powder products because it may be contaminated with Salmonella.
Voluntary / mandated
Voluntary: Firm initiated
Product description
ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tamarack Inc. Cheyenne, WY
Distribution pattern
Distributed to retail stores in Utah. No foreign/VA/govt/military consignees.
Recall initiation date
Mar 19, 2018
Initial firm notification
Visit
Center classification date
Apr 4, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0992-2018, published Apr 11, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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